1. Shaping Our Minds: Stem and Progenitor Cell Diversity in the Mammalian Neocortex 
Santos J. Franco, Ulrich Müller 
Neuron 
Volume 77, Issue 1, Pages (January 2013)
DOI: /j.neuron
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2. Figure 1
Major Subtypes of Neocortical Projection Neurons, Classified by Projection Pattern and Laminar Position
(A) Sagittal view of corticofugal projection neurons in lower layers. Corticothalamic neurons are found mostly in layer VI and project to the thalamus. Subcerebral projection neurons are located in the lower parts of layer V and send primary projections to the spinal cord, pons and superior colliculus.
(B) Coronal view of corticocortical projection neurons in upper layers. Most ipsilateral and callosal projection neurons are located in layers II–III and project within the same hemisphere or to the contralateral hemisphere via the corpus callosum, respectively. A subset of callosal neurons is also found in the superficial parts of layer V (not shown). Columnar projection neurons are found in layer IV and send short axons locally within a neocortical column.
(C) Magnified view of projection neuron subtypes represented in (A) and (B), detailing the relationships between laminar positions and projection patterns.
Neuron  , 19-34DOI: ( /j.neuron )
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3. Figure 2
Different Models of Projection Neuron Cell-Type Specification in the Developing Neocortex
(A) A single kind of RGC progenitor sequentially generates all subtypes of projection neurons and macroglia. The fate potential of the common RGC is progressively restricted over time; thus, projection neuron subtype identity is specified by birth date.
(B) Distinct subtypes of RGC progenitors co-exist and are pre-specified to generate different subtypes of projection neurons and macroglia. Projection neuron subtype fate is therefore specified by progenitor type, rather than by birth date.
VZ, ventricular zone; SVZ, subventricular zone; LL, lower layers; UL, upper layers; MZ, marginal zone.
Neuron  , 19-34DOI: ( /j.neuron )
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4. Figure 3
Subtypes of Stem and Progenitor Cells in the Developing Neocortex
Early in neocortical development, neuroepithelial cells divide symmetrically to expand the progenitor pool before transforming into radial glial cells (RGCs). RGCs typically divide asymmetrically to self-renew and produce either neurons or intermediate progenitor cells (IPCs). IPCs divide symmetrically to generate pairs of neurons, or in some cases additional IPCs that then make neurons. Short neural precursors are similar to IPCs in that they undergo terminal symmetric divisions to make neurons, but like RGCs they maintain an apical end foot and are located in the ventricular zone. Basal RGCs (bRGCs) have a basal attachment at the pial basement membrane similar to RGCs, but do not maintain an apical process and thus have their cell bodies located in the outer margins of the SVZ. bRGCs self-renew (not shown) and generate IPCs and neurons. At the end of neurogenesis, RGCs and bRGCs transform into astrocyte progenitors. For abbreviations, see legend to Figure 2.
Neuron  , 19-34DOI: ( /j.neuron )
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5. Figure 4
Distinct Lineages of Fate-Restricted RGCs Generate Lower- versus Upper-Layer Projection Neurons
(A) Corticofugal projection neurons in lower layers V–VI are generated from Cux2− RGCs that are neurogenic during early stages of neocortical development. Corticocortical projection neurons in upper layers II–IV are made from Cux2+ RGCs that coexist with Cux2− RGCs during early stages of neocortical development, but are initially proliferative and only become neurogenic at later developmental stages.
(B and C) Hypothetical lineage trees for the different subtypes of neocortical projection neurons. In both models, neuroepithelial cells transform into RGCs, which are then specified into the Cux2+ and Cux2− lineages. In (B), Cux2+ and Cux2− RGCs are then progressively restricted over time to sequentially generate the different projection neuron subtypes based on birth date. In (C), progenitors of the two lineages undergo further specification at the progenitor state to generate additional lineages of fate-restricted RGCs that produce a specific projection neuron subtype.
For abbreviations see legend to Figure 2.
Neuron  , 19-34DOI: ( /j.neuron )
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6. Figure 5 Signals that Control RGC Proliferative Behavior
A number of signaling molecules that are secreted by the meninges or that are present in the cerebrospinal fluid can act on RGCs to regulate their proliferative and neurogenic behaviors. Similarly, IPCs and neurons secrete signals that provide a feedback mechanism for controlling the balance between proliferation and neurogenesis in RGCs.
Neuron  , 19-34DOI: ( /j.neuron )
Copyright © 2013 Elsevier Inc. Terms and Conditions